Compared with other well-established knee designs, the uncemented rotating platform ATTUNE knee system has similar outcomes regarding survivorship and complications, but may have improved early recovery.
ID
Bron
Verkorte titel
Aandoening
Knee Osteoarthritis
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Survivorship: Calculated by determining revision rate. Septic, aseptic and all-cause revision rates will be calculated seperately.
Complication rate: All substantial complications associated with total knee arthroplasty will be registered and reported
Forgotten Joint Score 12 (FJS-12)
Kujala Anterior Knee Pain Scale (AKPS)
Knee injury and Osteoarthritis Outcome Scale - Physical Function Short Form
KOOS-PS
Numeric Rating Scale (NRS): NRS on pain and satisfaction
EuroQol 5 Dimensions, 3 Levels (EQ5D-3L)
Achtergrond van het onderzoek
To accomodate dissatisfied patients with a total knee arthroplasty (TKA) and improve outcomes, several knee systems have been developed. The cemented ATTUNE TKA shows superiority over other established knee systems at short-term, abating with longer follow-up. There have been no studies reporting on the results of the uncemented version of the ATTUNE. Therefore, the main objective of the current study was to report patient reported outcome measures (PROMs), survivorship and complications associated with the uncemented ATTUNE TKA.
Doel van het onderzoek
Compared with other well-established knee designs, the uncemented rotating platform ATTUNE knee system has similar outcomes regarding survivorship and complications, but may have improved early recovery.
Onderzoeksopzet
1 year, 5 years and 10 years
Onderzoeksproduct en/of interventie
Total knee arthroplasty (TKA) with the uncemented ATTUNE rotating platform.
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
End-stage osteoarthritis of the knee warranting joint replacement therapy.
Indicated for an ATTUNE total knee system as part of regular clinical practice.
Capability and willingness to sign informed consent and comply with follow-up procedures.
Capable enough in Dutch or English to be able to understand study procedures
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Unable or unwilling to sign informed consent and comply with follow-up
Indication for primary revision arthroplasty
Absolute indication for cemented fixation (decreased bone stock/quality of spongiosa)
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL8929 |
| CCMO | NL71274.029.19 |
| OMON | NL-OMON55973 |